3DP Lumbar Interbody System

Primary DI
M719GP3D1332L80
Brand
3DP Lumbar Interbody System
Company
Genesys Orthopedics Systems LLC
Model
1
Catalog number
GP3D-1332L8
Device description
13mm x 32mm 8 deg Lordotic 3DP TPLIF
Published
2025-08-21
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
MAXIntervertebral Fusion Device With Bone Graft, LumbarOrthopedic2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K182987000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K182987000Genesys Spine 3DP Lumbar Interbody SystemGenesys Spine2019-12-12MAX

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
M719GP3D1332L80PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Metallic spinal interbody fusion cageA device intended to be implanted into the space of an intervertebral disc that has been partially or totally removed during surgery in order to allow bone fusion between two contiguous vertebral bodies, typically in the treatment of degenerative disc disease (DDD). It is typically in the form of a hollow, porous, threaded and/or fenestrated cylindrical, or disc-shaped device made of metal [e.g., titanium (Ti)] that provides mechanical stability and sufficient space for therapeutic spinal bone fusion to occur; bone graft is typically used to help with osseointegration. Fixation screws and devices associated with implantation may be packaged with the cage.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
5123817089info@genesysspine.com

Regulatory Flags#

DUNS number
017921066
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
M719G120000SIros-X1G120002026-08-03
M719G120010SIros-X1G120012026-08-03
M719G120020SIros-X1G120022026-08-03
M719G120030SIros-X1G120032026-08-03
M719G120040SIros-X1G120042026-08-03
M719G45170Stasys-C Standalone1G45172026-08-03
M719G45180Stasys-C Standalone1G45182026-08-03
M719GL3110TiLock1GL3112026-08-03
M719GLC403S0TiLock1GLC403-S2026-08-03
M719GSIX1260SIros-X1GSI-X1262026-08-03
M719G120140SIros-X1G120142026-07-14
M719G45120Apache1G45122018-12-14
M719GAC1020Apache1GAC1022018-12-14
M719G45150Apache AIS-C Standalone1G45152023-07-24
M719G45160Apache AIS-C Standalone1G45162023-07-24
M719GL201TL0SIros-X1GL201T-L2026-07-23
M179GSI265STS0Sacroiliac Joint Fusion1GSI265-ST-S2026-07-14
M719GGSI265XLGS0Sacroiliac Joint Fusion1GSI265-XLG-S2026-07-14
M719GL2290TiLock1GL2292026-07-14
M719GLL100QC03DP Lumbar Interbody System1GLL100-QC2026-07-14

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00843511102838Omnia Medical TiBrid™-TSOMNIA MEDICAL, LLCMAX2026-08-03
00843511102845Omnia Medical TiBrid™-TSOMNIA MEDICAL, LLCMAX2026-08-03
00810166521604X-PACEXPANDING INNOVATIONS, INC.MAX2026-07-30
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